Associated Papers
De novo variants in KDM2A cause a syndromic neurodevelopmental disorder.
Anderson EN et al.
American Journal of Human Genetics, 2026
41468891 (PubMed )
Supplement: mmc2.xlsx › S7_KDM_genes_literature
Genotype-phenotype correlation study of structural abnormalities in a fetal brain caused by a novel KDM4B variant.
Zhao X et al.
Molecular Biology Reports, 2024
AutoCaSc: Prioritizing candidate genes for neurodevelopmental disorders.
Lieberwirth JK et al.
Human Mutation, 2022
Whole genome sequencing of Malaysian colorectal cancer patients reveals specific druggable somatic mutations.
Mohd Yunos RI et al.
Frontiers in Molecular Biosciences, 2022
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